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Technical Writer - Assay Development
Software Guidance & Assistance, Inc., (SGA), is searching for a
Technical Writer - Assay Development
for a
contract
assignment with one of our premier Pharmaceutical services clients in
Tucson, AZ .
Responsibilities
Act as the Technical Writer on project teams, attend meetings, and update the supervisor.
Involved in the creation, review, revision, and approval of documentation and labeling for the firm's Tissue Diagnostics products.
Required Skills
Bachelor's degree in a scientific discipline or other related technical field.
3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry.
Knowledge of current US and international regulations (e.g., FDA, ISO, IVDD, 21 CFR 11) and control of electronic records.
Demonstrable record of working on project teams while managing multiple projects.
Preferred Skills
Experience with international regulatory requirements.
Equal Opportunity Statement SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or other legally protected status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities.
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Technical Writer - Assay Development
for a
contract
assignment with one of our premier Pharmaceutical services clients in
Tucson, AZ .
Responsibilities
Act as the Technical Writer on project teams, attend meetings, and update the supervisor.
Involved in the creation, review, revision, and approval of documentation and labeling for the firm's Tissue Diagnostics products.
Required Skills
Bachelor's degree in a scientific discipline or other related technical field.
3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry.
Knowledge of current US and international regulations (e.g., FDA, ISO, IVDD, 21 CFR 11) and control of electronic records.
Demonstrable record of working on project teams while managing multiple projects.
Preferred Skills
Experience with international regulatory requirements.
Equal Opportunity Statement SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or other legally protected status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities.
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